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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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NeoGen® PTFE Membrane, Ti-Reinforced - M I
Neoss AB
64011
In Commercial Distribution

  • 05060440330933 ()
64011

  • Pliable-polymer dental regeneration membrane, non-bioabsorbable
NeoGen® PTFE Membrane, Ti-Reinforced - S I
Neoss AB
64010
In Commercial Distribution

  • 05060440330926 ()
64010

  • Pliable-polymer dental regeneration membrane, non-bioabsorbable
Access Ball Abutment 1.0 mm
Neoss AB
31334
In Commercial Distribution

  • 05060440330902 ()
31334

  • Dental implant suprastructure, permanent, preformed
Access Provisional Ti Abutment Multi
Neoss AB
31301
In Commercial Distribution

  • 05060440330827 ()
31301

  • Screw endosteal dental implant, two-piece
Implant Kit - ProActive Ø6.0 x 11 mm
Neoss AB
21251
In Commercial Distribution

  • 05060440330537 ()
21251

  • Screw endosteal dental implant, two-piece
Implant Kit - ProActive Ø6.0 x 9 mm
Neoss AB
21250
In Commercial Distribution

  • 05060440330520 ()
21250

  • Screw endosteal dental implant, two-piece
Implant Kit - ProActive Tapered Ø5.5 x 13 mm
Neoss AB
21247
In Commercial Distribution

  • 05060440330513 ()
21247

  • Screw endosteal dental implant, two-piece
Implant Kit - ProActive Tapered Ø5.5 x 11 mm
Neoss AB
21246
In Commercial Distribution

  • 05060440330506 ()
21246

  • Screw endosteal dental implant, two-piece
Implant Kit - ProActive Tapered Ø5.5 x 9 mm
Neoss AB
21245
In Commercial Distribution

  • 05060440330490 ()
21245

  • Screw endosteal dental implant, two-piece
Implant Kit - ProActive Tapered Ø5.0 x 15 mm
Neoss AB
21242
In Commercial Distribution

  • 05060440330483 ()
21242

  • Screw endosteal dental implant, two-piece
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